Osteogenic Differentiation of Mesenchymal Stromal Cells: A Comparative Analysis Between Human Subcutaneous Adipose Tissue and Dental Pulp

被引:22
作者
D'Alimonte, Iolanda [1 ,3 ,4 ,5 ]
Mastrangelo, Filiberto [6 ]
Giuliani, Patricia [1 ]
Pierdomenico, Laura [2 ,3 ,4 ,5 ]
Marchisio, Marco [2 ,3 ,4 ,5 ]
Zuccarini, Mariachiara [1 ,3 ,4 ]
Di Iorio, Patrizia [1 ]
Quaresima, Raimondo [7 ]
Caciagli, Francesco [1 ]
Ciccarelli, Renata [1 ,3 ,4 ,5 ]
机构
[1] Univ G dAnnunzio, Dept Med Oral & Biotechnol Sci, Chieti, Italy
[2] Univ G dAnnunzio, Dept Med & Aging Sci, Chieti, Italy
[3] Univ G dAnnunzio, Aging Res Ctr, Chieti, Italy
[4] Univ G dAnnunzio, Translat Med CeSI MeT, Chieti, Italy
[5] StemTeCh Grp, Chieti, Italy
[6] Vita & Salute Univ, IRCCS San Raffaele Sci Inst, Unit Dent, Milan, Italy
[7] Univ Aquila, Dept Civil Engn Architecture & Environm, Laquila, Italy
关键词
regenerative medicine; mesenchymal stromal cells from human subcutaneous adipose tissue (S-ASCs); characteristics of the osteogenic differentiation of S-ASCs; UMBILICAL-CORD BLOOD; STEM-CELLS; BONE-MARROW; IN-VITRO; PROLIFERATION; REGENERATION; OSTEOBLASTS; EXPRESSION; STRATEGIES; THERAPY;
D O I
10.1089/scd.2016.0190
中图分类号
Q813 [细胞工程];
学科分类号
摘要
White adipose tissue is a source of mesenchymal stromal/stem cells (MSCs) that are actively studied for their possible therapeutic use in bone tissue repair/remodeling. To better appreciate the osteogenic potential of these cells, we compared some properties of MSCs from human subcutaneous adipose tissue [subcutaneous-adipose stromal cells (S-ASCs)] and dental pulp stem cell (DPSCs) of third-impacted molars, the latter representing a well-established MSC source. Both undifferentiated cell types showed similar fibroblast-like morphology and mesenchymal marker expression. However, undifferentiated S-ASCs displayed a faster doubling time coupled to greater proliferation and colony-forming ability than DPSCs. Also, the osteogenic differentiation of S-ASCs was greater than that of DPSCs, as evaluated by the higher levels of expression of early osteogenic markers Runt-related transcription factor-2 (RUNX2) and alkaline phosphatase at days 3-14 and of extracellular matrix mineralization at days 14-21. Moreover, S-ASCs showed a better colonization of the titanium scaffold. In addition, we investigated whether S-ASC osteogenic commitment was enhanced by adenosine A1 receptor (A1R) stimulation, as previously shown for DPSCs. Although A1R expression was constant during DPSC differentiation, it increased in S-ASC at day 21 from osteogenesis induction. Accordingly, A1R stimulation by the agonist 2-chloro-N-6-cyclopentyladenosine, added to the cultures at each medium change, stimulated proliferation only in differentiating DPSC and enhanced the osteogenic differentiation earlier in DPSCs than in S-ASCs. These effects were counteracted by cell pretreatment with a selective A1R antagonist. Thus, our findings suggest that S-ASCs could be advantageously used in regenerative orthopedics/dentistry, and locally released or exogenously added purines may play a role in bone repair/remodeling, even though this aspect should be more thoroughly evaluated.
引用
收藏
页码:843 / 855
页数:13
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